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Philip Stanier

Showing results (31-40 of 69) with videos related to

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Human Molecular Genetics|August 28, 2007
Increased expression of Grainyhead-like-3 rescues spina bifida in a folate-resistant mouse modelPeter Gustavsson, Nicholas D E Greene, Dina Lad, et al.
Human Molecular Genetics|September 11, 2019
Exome sequencing identifies variants in FKBP4 that are associated with recurrent fetal loss in humansCharalambos Demetriou, Estelle Chanudet, , et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 16, 2004
Imprinted methylation profiles for proximal mouse chromosomes 11 and 7 as revealed by methylation-sensitive representational difference analysisDavid Monk, Rachel Smith, Philippe Arnaud, et al.
Human Molecular Genetics|August 4, 2009
Tbx22null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypesErwin Pauws, Aya Hoshino, Lucy Bentley, et al.
Scientific Reports|February 22, 2018
Spina bifida-predisposing heterozygous mutations in Planar Cell Polarity genes and Zic2 reduce bone mass in young miceIsabel R Orriss, Stuart Lanham, Dawn Savery, et al.
Epigenetics|September 25, 2010
The effects of culture on genomic imprinting profiles in human embryonic and fetal mesenchymal stem cellsJennifer Frost, Dave Monk, Dafni Moschidou, et al.
Human Molecular Genetics|December 25, 2002
Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouseJennifer N Murdoch, Deborah J Henderson, Kit Doudney, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 7, 2003
DDC and COBL, flanking the imprinted GRB10 gene on 7p12, are biallelically expressedMegan P Hitchins, Louise Bentley, David Monk, et al.
Genome Research|May 16, 2008
Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-silencingDavid Monk, Alexandre Wagschal, Philippe Arnaud, et al.
American Journal of Human Genetics|September 12, 2007
TBX22 missense mutations found in patients with X-linked cleft palate affect DNA binding, sumoylation, and transcriptional repressionArtemisia M Andreou, Erwin Pauws, Marius C Jones, et al.
Pageof 7

Showing results (31-40 of 69) with videos related to

Sort By:
Pageof 7
Human Molecular Genetics|August 28, 2007
Increased expression of Grainyhead-like-3 rescues spina bifida in a folate-resistant mouse modelPeter Gustavsson, Nicholas D E Greene, Dina Lad, et al.
Human Molecular Genetics|September 11, 2019
Exome sequencing identifies variants in FKBP4 that are associated with recurrent fetal loss in humansCharalambos Demetriou, Estelle Chanudet, , et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 16, 2004
Imprinted methylation profiles for proximal mouse chromosomes 11 and 7 as revealed by methylation-sensitive representational difference analysisDavid Monk, Rachel Smith, Philippe Arnaud, et al.
Human Molecular Genetics|August 4, 2009
Tbx22null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypesErwin Pauws, Aya Hoshino, Lucy Bentley, et al.
Scientific Reports|February 22, 2018
Spina bifida-predisposing heterozygous mutations in Planar Cell Polarity genes and Zic2 reduce bone mass in young miceIsabel R Orriss, Stuart Lanham, Dawn Savery, et al.
Epigenetics|September 25, 2010
The effects of culture on genomic imprinting profiles in human embryonic and fetal mesenchymal stem cellsJennifer Frost, Dave Monk, Dafni Moschidou, et al.
Human Molecular Genetics|December 25, 2002
Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouseJennifer N Murdoch, Deborah J Henderson, Kit Doudney, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 7, 2003
DDC and COBL, flanking the imprinted GRB10 gene on 7p12, are biallelically expressedMegan P Hitchins, Louise Bentley, David Monk, et al.
Genome Research|May 16, 2008
Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-silencingDavid Monk, Alexandre Wagschal, Philippe Arnaud, et al.
American Journal of Human Genetics|September 12, 2007
TBX22 missense mutations found in patients with X-linked cleft palate affect DNA binding, sumoylation, and transcriptional repressionArtemisia M Andreou, Erwin Pauws, Marius C Jones, et al.
Pageof 7